Research Nurse

Guy's and St Thomas' NHS Foundation Trust

This job is now closed

Job summary

We are looking for an enthusiastic band 6 research nurse to join the cardio-oncology team at Royal Brompton Hospital. This is a newly created post to support cardio-oncology research projects within the new centre of excellence of cardio-oncology at Royal Brompton Hospital. You will work closely with the cardio-oncology consultants and clinical nurse specialist along with the wider research team at Royal Brompton.

Main duties of the job

The function of a clinical research nurse is to support a portfolio of cardiovascular clinical studies in Royal Brompton and Harefield hospitals for the Cardio-Oncology Centre of Excellence. You will be responsible for assessing and managing the care pathways for patients and carers participating in clinical trials, be directly involved in the recruitment, education and monitoring of trial patients and in the collection and documentation of accurate data.

About us

Royal Brompton & Harefield hospitals make up the largest specialist heart and lung centre in the UK and is among the largest in Europe. We are part of the Heart, Lung, and Critical Care clinical group within Guy's and St Thomas' NHS Foundation Trust which is known for its expertise, standard of care and research success.

Date posted

18 October 2024

Pay scheme

Agenda for change

Band

Band 6

Salary

£44,806 to £53,134 a year per annum incl. HCA

Contract

Fixed term

Duration

1 years

Working pattern

Full-time

Reference number

196-RD169

Job locations

Royal Brompton hospital

Sydney Street

london

SW3 6NP

Job description

Job responsibilities

The post-holder will:

Assist senior research staff in the day-to-day running of research projects, caring for research patients, and liaising with other departments and external agencies.
Obtain informed consent for research projects, including genetic research, ensuring the following is accounted for:

The patient (and significant others) fully understand the nature of the clinical trial.
The patient is aware that entry into the trial is voluntary and they can withdraw at any point without prejudice.
The patient is aware of any extra procedures required by the trial.
The consent form is completed accurately and filed as required.

Collect and process blood and other samples from patients for research projects.
Maintain and regularly update databases on patients records and outcomes, including associated administrative tasks such as writing to patients or their medical teams
Assist in the management, coordination, organisation and implementation of basic science and clinical trial protocols in accordance with International Conference on Harmonisation/ Good Clinical Practice (ICH/GCP). This would be for both non-commercial and commercial studies
Use appropriate manual and computerized systems, and ensure accurate collection and maintenance of all study records, including the backing up of data.
Supervise and assist in the development of local Standard Operating Procedures (SOPs).
Facilitate effective communication of complex study information with all relevant research personnel, including medical, nursing, administrative, and pharmacy staff.
Identify strategies and take responsibility for the recruitment of patients into clinical studies at the RBHT to which you are allocated.
Identify barriers to recruitment to trials and ensure that the site PI and Research Office are made aware of them. Identify and implement action/plans as required.
Ensure that clinical trial protocols are adhered to.
Ensure that you and the teams on the clinical trials to which you are assigned are working according to GCP, HTA, and research governance standards for clinical trials.
Supply data as required to the RBHT Research Office and the South London CRN regarding progress of clinical trials.

Job description

Job responsibilities

The post-holder will:

Assist senior research staff in the day-to-day running of research projects, caring for research patients, and liaising with other departments and external agencies.
Obtain informed consent for research projects, including genetic research, ensuring the following is accounted for:

The patient (and significant others) fully understand the nature of the clinical trial.
The patient is aware that entry into the trial is voluntary and they can withdraw at any point without prejudice.
The patient is aware of any extra procedures required by the trial.
The consent form is completed accurately and filed as required.

Collect and process blood and other samples from patients for research projects.
Maintain and regularly update databases on patients records and outcomes, including associated administrative tasks such as writing to patients or their medical teams
Assist in the management, coordination, organisation and implementation of basic science and clinical trial protocols in accordance with International Conference on Harmonisation/ Good Clinical Practice (ICH/GCP). This would be for both non-commercial and commercial studies
Use appropriate manual and computerized systems, and ensure accurate collection and maintenance of all study records, including the backing up of data.
Supervise and assist in the development of local Standard Operating Procedures (SOPs).
Facilitate effective communication of complex study information with all relevant research personnel, including medical, nursing, administrative, and pharmacy staff.
Identify strategies and take responsibility for the recruitment of patients into clinical studies at the RBHT to which you are allocated.
Identify barriers to recruitment to trials and ensure that the site PI and Research Office are made aware of them. Identify and implement action/plans as required.
Ensure that clinical trial protocols are adhered to.
Ensure that you and the teams on the clinical trials to which you are assigned are working according to GCP, HTA, and research governance standards for clinical trials.
Supply data as required to the RBHT Research Office and the South London CRN regarding progress of clinical trials.

Person Specification

education and qualifications

Essential

NMC registration
evidence of ongoing professional development

Desirable

specialist qualification
qualification in teaching and mentorship

Knowledge and experience

Essential

relevant post registration experience

Desirable

clinical research experience

skills and abilities

Essential

ability to work independently
excellent interpersonal, communication and organisation skills
able to prioritise and deliver objectives

Person Specification

education and qualifications

Essential

NMC registration
evidence of ongoing professional development

Desirable

specialist qualification
qualification in teaching and mentorship

Knowledge and experience

Essential

relevant post registration experience

Desirable

clinical research experience

skills and abilities

Essential

ability to work independently
excellent interpersonal, communication and organisation skills
able to prioritise and deliver objectives

Disclosure and Barring Service Check

This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

Certificate of Sponsorship

Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).

From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).